| Literature DB >> 30388155 |
Nick Verhaeghe1,2, Janne Schepers1,3, Patrick van Dun4, Lieven Annemans1.
Abstract
The aim of the current study was to evaluate the literature examining the impact of osteopathic care for spinal complaints. The bibliographic databases Medline (Pubmed), Web of Science, Embase, and PEDro were searched. In addition, a number of grey literature sources were searched. Only randomized controlled trials conducted in high-income Western countries were considered. Two authors independently screened the titles and abstracts. Primary outcomes included 'pain' and 'functional status', while secondary outcomes included 'medication use' and 'health status'. It was examined if differences existed related to the treatment protocol and geography (European vs. US studies). Study quality was assessed using the risk of bias tool of the Cochrane Back Review Group. Nineteen studies were included and qualitatively synthesized. Nine studies were from the US, followed by Germany with seven studies. The majority of studies (n = 13) focused on low back pain. In general, mixed findings related to the impact of osteopathic care on primary and secondary outcomes were observed. For the primary outcomes, a clear distinction between US and European studies was found, in favor of the latter ones. Studies were characterized by substantial methodological differences in sample sizes, number of treatments, control groups, and follow-up. In conclusion, there is some evidence suggesting that osteopathic care may be effective for people suffering from spinal complaints. Further studies with larger study samples and assessment of long-term impact are required to further increase the evidence-based knowledge of the potential of osteopathic care for individuals suffering from spinal complaints.Entities:
Mesh:
Year: 2018 PMID: 30388155 PMCID: PMC6214527 DOI: 10.1371/journal.pone.0206284
Source DB: PubMed Journal: PLoS One ISSN: 1932-6203 Impact factor: 3.240
Fig 1Flow chart of the study selection process.
Eligibility criteria.
| PICOS | inclusion criteria | exclusion criteria |
|---|---|---|
| individuals with back pain, LBP, neck pain, pelvic girdle pain–no age restrictions | individuals suffering from other than spinal complaints | |
| care administered by an osteopathic practitioner | care performed by other professionals | |
| no intervention, sham/placebo, or usual care (no restrictions on definition of usual care) | NA | |
| pain, functional status, medication use, health status | other outcomes | |
| randomized controlled trials | other study designs | |
| English, French, Dutch, German | other languages | |
| published from 1/1/1995–31/01/2017 (Pubmed & Web of Science) | published prior to 1/1/1995 and after 31/01/2017 | |
| high-income Western countries | other |
LBP, low back pain; NA, not applicable
Overview of characteristics of included studies.
| first author (year) | country | study population | osteopathic intervention | intervention duration | follow-up |
|---|---|---|---|---|---|
| Andersson (1999) | US | patients 20-59y LBP ≥3w-≤6m | custom tailored | 12w (8 sessions) | NA |
| Licciardone (2003) | US | patients 21-69y non-specific LBP ≥3m | custom tailored | 5m (7 sessions) | 4w |
| UK BEAM (2004) | UK | patients LBP | semi-standardized | 12w (8 sessions) | 9m |
| McReynolds (2005) | US | patients neck pain <3w | semi-standardized | one session | NA |
| Peters (2006) | Germany | pregnant (20-30w) women LBP | custom tailored | 4w (4 sessions) | NA |
| Heinze (2006) | Germany | patients 18-65y LBP ≥3w-≤6m | custom tailored | 6w (2–3 sessions) | 6w |
| Chown (2008) | UK | patients 18-65y >3m simple LBP | semi-standardized | 3m (5 sessions) | 9m |
| Recknagel (2008) | Germany | women 18-46y post-partum BP ≥3m-≤24m | custom tailored | 6w (4 sessions) | 6w |
| Schwerla (2008) | Germany | patients 20-55y ≥3m non-specific neck pain | custom tailored | 10w (5 sessions) | 3m |
| Engemann (2009) | Germany | patients 18-60y chronic non-specific neck pain | custom tailored | 6 sessions | 3m |
| Licciardone (2010) | US | pregnant women (≤30w) BP | semi-standardized | 10w (7 sessions) | NA |
| Cruser (2012) | US | military staff 18-35y acute LBP | semi-standardized | 4w (4 sessions) | 4w |
| Vismara (2012) | Italy | obese females (BMI>30kg/m2chronic LBP >6m | semi-standardized | 10 sessions | NA |
| Licciardone (2013a) | US | diabetes mellitus patients 21-69y LBP | semi-standardized | 8w (6 sessions) | 4w |
| Licciardone (2013b) | US | non-pregnant adults 21-69y LBP ≥3m | semi-standardized | 8w (6 sessions) | 4w |
| Belz (2015) | Germany | women 18-42y post-partum non-specific BP ≥3m | custom tailored | 10w (5 sessions) | 3m |
| Hensel (2015) | US | pregnant (30w) women 18-35y LBP | standardized | 10w (7 sessions) | NA |
| Schwerla (2015) | Germany | women 18-42y post-partum LBP or pelvic girdle pain ≥3m | custom tailored | 6w (4 sessions) | 2w |
| Licciardone (2016) | US | patients 21-69y non-specific LBP ≥3m | semi-standardized | 8w (6 sessions) | 4w |
*time period starting after the last treatment session
**no information on intervention duration provided
BP, back pain; LBP, low back pain; m, months; NA, not applicable; w, weeks; y, year
Overview of intervention and control groups, outcome measurements and main findings.
| first author (year) | intervention + n° of participants | control + n° of participants | outcome measurement | findings intervention vs. control |
|---|---|---|---|---|
| Andersson (1999) | OT + SAT (n = 83) | SAT (n = 72) | pain: VAS; functional status: RMDQ/OPQ | |
| Licciardone (2003) | OT (n = 48) | sham manipulation (n = 23) no intervention (n = 20) | pain: VAS, functional status: RMDQ | |
| UK Beam (2004) | OT+best care | best care | functional status: RMDQ | OT+best care vs. best care: 3m, 1.57 [95%CI 0.82–2.32] p = 0.001; 12m, 1.01 [95%CI 0.22–1.81] p = 0.05 / OT+best care+ exercise vs. best care: 3m, 1.87 [95%CI 1.15–2.60] p = 0.001; 12m, 1.30 [95%CI 0.54–2.07] p = 0.01 |
| McReynolds (2005) | OT (n = 29) | medication (n = 29) | pain: NRS/PRS | 2.8±1.7 vs. 1.7±1.6 (p = 0.02); |
| Peters (2006) | OT (n = 30) | no intervention (n = 30) | pain: VAS; functional status: QBPDS | |
| Heinze (2006) | OT + heat + physiotherapy (n = 28) | heat + physiotherapy (n = 32) | pain: NRS; functional status: RMDQ | |
| Chown (2008) | OT (n = 79) | physiotherapy (n = 80) | functional status: ODI | mean score OT, -5.0 [95%CI -1.6, -8.4] p<0.01; PT, -4.1 [95%CI -1.4, -6.9] p<0.01 |
| Schwerla (2008) | OT + sham UST (n = 23) | UST (n = 18) | pain: NRS | average pain, 2.48 vs. 0.75 difference: -1.73 [95%CI -3.13, -0.32] p = 0.017 / OT: significant decrease in actual (p = 0.001) and worst (p = 0.001) pain |
| Recknagel (2008) | OT (n = 20) | no intervention (n = 19) | pain: VAS; functional status: OPQ | |
| Engemann (2009) | OT (n = 15) | no intervention (n = 15) | pain: NPAD/NRS | -2.14 vs. 0.32 (p<0.001) |
| Licciardone (2010) | OT + UOC (n = 49) | UOC + sham UST (n = 48) / UOC (n = 49) | pain: VAS; functional status: RMDQ | |
| Cruser (2012) | OT + UC (n = 30) | UC (n = 30) | pain: VAS; functional status: RMDQ | |
| Vismara (2012) | OT + exercise (n = 10) | exercise (n = 11) | pain: VAS; functional status: RMDQ/ODI | |
| Licciardone (2013a) | OT + (sham) UST (n = 19) | shamOT+(sham)UST(n = 15) | pain: VAS | difference 1.7 [95%CI 3.2, 0.1] p = 0.04 |
| Licciardone (2013b) | OT + (sham) UST (n = 230) | sham OT + (sham) UST (n = 225) | pain: VAS; functional status: RMDQ | |
| Hensel (2015) | OT (n = 136) | placebo UST (n = 131) / UOC (n = 133) | pain: VAS; functional status: RMDQ | |
| Belz (2015) | OT (n = 30) | no intervention (n = 30) | pain: VAS; functional status: PGQ | |
| Schwerla (2015) | OT (n = 40) | no intervention (n = 40) | pain: VAS; functional status: ODI | |
| Licciardone (2016) | OT (n = 175) | sham OT (n = 170) | pain: VAS; functional status: RMDQ |
*based on the UK national acute back pain guidelines 'continuing normal activities and avoiding rest' / IQR, interquartile range; NPAD, Neck Pain and Disability Scale; NRS, Numerical Rating Scale
ODI, Oswestry Disability Index; OPQ, Oswestry Pain Questionnaire; OT, osteopathic treatment; PGQ, Pelvic Girdle Pain Questionnaire; PRS, Pain Relief Scale; QBPDS, Quebec Back Pain Disability Scale; RMDQ, Roland-Morris Disability Questionnaire; RR, response ratio; SAT, standard allopathic treatment; UC, usual care; UOC, usual obstetrical care; UST, ultrasound treatment; VAS, Visual Analogue Scale
Effectiveness of osteopathic care related to the outcome ‘pain’.
| Study | Treatment protocol | treatment effect | |||
|---|---|---|---|---|---|
| OT worse than controls | non-significant improvement OT | signif. improvement OT/no signif. between-group difference | significant between-group difference | ||
| Peters (2006) | custom | x | |||
| Heinze (2006) | custom | x | |||
| Recknagel (2008) | custom | x | |||
| Schwerla (2008) | custom | actual & worst pain | average pain | ||
| Engemann (2009) | custom | x | |||
| Schwerla (2015) | custom | x | |||
| Belz (2015) | custom | x | |||
| Vismara (2012) | semi-standardized | x | |||
| Andersson (1999) | custom | x | |||
| Licciardone (2003) | custom | OT vs. sham | OT vs. control | ||
| McReynolds (2005) | semi-standardized | pain relief | pain intensity | ||
| Cruser (2012) | semi-standardized | x | |||
| Licciardone (2013a) | semi-standardized | x | |||
| Licciardone (2013b) | semi-standardized | x | |||
| Hensel (2015) | semi-standardized | OT vs. PUT | OT vs. UOC | ||
| Licciardone (2016) | semi-standardized | x | |||
| Licciardone (2010) | standardized | x | |||
OT, osteopathic treatment; PUT, placebo ultrasound treatment; UOC, usual obstetrical care
Effectiveness of osteopathic care related to the outcome ‘functional status’.
| Study | Treatment protocol | treatment effect | |||
|---|---|---|---|---|---|
| OT worse than controls | non-significant improvement OT | signif. improvement OT/no signif. between-group difference | significant between-group difference | ||
| Peters (2006) | custom | x | |||
| Heinze (2006) | custom | x | |||
| Recknagel (2008) | custom | x | |||
| Schwerla (2015) | custom | x | |||
| Belz (2015) | custom | x | |||
| UK BEAM (2004) | semi-standardized | x | |||
| Chown (2008) | semi-standardized | x | |||
| Vismara (2012) | semi-standardized | x | |||
| Andersson (1999) | custom | x | |||
| Licciardone (2003) | custom | x | |||
| Cruser (2012) | semi-standardized | x | |||
| Licciardone (2013b) | semi-standardized | x | |||
| Hensel (2015) | semi-standardized | OT vs. PUT | OT vs. UOC | ||
| Licciardone (2016) | semi-standardized | x | |||
| Licciardone (2010) | standardized | x | |||
OT, osteopathic treatment; PUT, placebo ultrasound treatment; UOC, usual obstetrical care
Risk of bias in the individual studies included in the review.
| first author (year) | randomi-zation? | allocation concealed? | patient blinding? | care provider blinding? | outcome assessor blinding? | drop-outs described & accepatble? | ITT-analysis? | free of suggestion of selective outcome reporting? | groups similar at baseline? | co-interventions avoided or similar? | acceptable compliance? | similar timing outcome assessment? | yes-score |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Andersson (1999) | yes | yes | no | no | no | no | no | yes | yes | yes | yes | yes | 7 |
| Licciardone (2003) | yes | yes | U | no | U | yes | U | no | yes | yes | U | yes | 6 |
| UK BEAM (2004) | yes | yes | no | no | no | yes | no | yes | yes | yes | yes | yes | 8 |
| McReynolds (2005) | yes | yes | no | no | no | yes | U | yes | yes | yes | NA | yes | 7 |
| Peters (2006) | yes | yes | no | no | no | yes | no | yes | yes | yes | yes | yes | 8 |
| Heinze (2006) | yes | yes | no | no | no | yes | yes | yes | no | yes | yes | yes | 8 |
| Chown (2008) | yes | yes | U | no | U | yes | U | yes | yes | yes | yes | yes | 8 |
| Recknagel (2008) | yes | yes | no | no | no | yes | yes | yes | yes | yes | yes | yes | 9 |
| Schwerla (2008) | yes | yes | no | no | no | yes | no | yes | yes | yes | U | yes | 7 |
| Engemann (2009) | yes | yes | no | no | no | yes | yes | yes | yes | yes | U | yes | 8 |
| Licciardone (2010) | yes | U | no | no | no | no | yes | yes | yes | yes | yes | yes | 7 |
| Cruser (2012) | yes | yes | no | no | no | yes | yes | yes | yes | yes | yes | yes | 9 |
| Vismara (2012) | yes | yes | no | no | no | yes | no | yes | yes | yes | yes | yes | 8 |
| Licciardone (2013a) | yes | yes | U | no | U | yes | no | no | yes | yes | U | yes | 6 |
| Licciardone (2013b) | yes | yes | U | no | U | yes | yes | no | yes | yes | yes | yes | 8 |
| Belz (2015) | yes | yes | no | no | no | yes | yes | yes | yes | yes | U | yes | 8 |
| Hensel (2015) | yes | yes | no | no | no | no | yes | yes | no | yes | no | yes | 6 |
| Schwerla (2015) | yes | yes | U | no | no | yes | yes | yes | no | yes | U | yes | 7 |
| Licciardone (2016) | yes | yes | U | no | U | yes | yes | yes | yes | yes | yes | yes | 9 |
*this criterion was scored ‘no’ if a significant between-group difference for at least one variable was present
**single-session intervention
ITT, intention-to-treat; NA, not applicable; U, unsure